Neuland Laboratories
NDC Database
Neuland Laboratories
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 65
- Latest Marketing Date 2026-05-18
- Data Source FDA
- First Marketing Date 2005-10-01
Company Overview
Social Profiles
Company Snapshot
Neuland Laboratories
11th Floor (5th Level), Phoenix IVY Building, Plot No. 573A-III, Road No. 82, Jubilee Hills, Hyderabad, 500033, Telangana
India
www.neulandlabs.com/en marketing@neulandlabs.com View on MapNDC Records ( 65 records )
Nonproprietary Name
ALBUTEROL SULFATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ALBUTEROL SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ofloxacin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
OFLOXACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Itraconazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ITRACONAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MIRTAZAPINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
MIRTAZAPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-13
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
OLANZAPINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
OLANZAPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ramipril
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
RAMIPRIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Enalapril Maleate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ENALAPRIL MALEATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levetiracetam
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LEVETIRACETAM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-03-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ropinirole Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ROPINIROLE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Escitalopram Oxalate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ESCITALOPRAM OXALATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Donepezil Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DONEPEZIL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dorzolamide Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DORZOLAMIDE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SALMETEROL XINAFOATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
SALMETEROL XINAFOATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SOTALOL HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
SOTALOL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PARICALCITOL
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PARICALCITOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MIRTAZAPINE ANHYDROUS
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
MIRTAZAPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LEVOFLOXACIN HEMIHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LEVOFLOXACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-10-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DAPIPRAZOLE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DAPIPRAZOLE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-10-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PALIPERIDONE PALMITATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PALIPERIDONE PALMITATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ROPINIROLE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ROPINIROLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-09-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sodium Phenyl Acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
SODIUM PHENYLACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-07-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
phenoxybenzamine hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PHENOXYBENZAMINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-11-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acetyl-Gly-Ala-Gln-Phe-Ser-Lys-Thr-Ala-Lys-OH. Acetate (BIO-11006)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
BIO-11006
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-10-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Posaconazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
POSACONAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-05-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Besifloxacin Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
BESIFLOXACIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ARIPIPRAZOLE LAUROXIL
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ARIPIPRAZOLE LAUROXIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-10-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PALIPERIDONE PALMITATE (STERILE)
Dosage Form
SOLUTION
Strength
1 mg/mg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PALIPERIDONE PALMITATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-10-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rotigotine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ROTIGOTINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-11-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
RABEPRAZOLE SODIUM MONOHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
RABEPRAZOLE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-10-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Indacaterol Maleate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
INDACATEROL MALEATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-11-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Donepezil Base
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DONEPEZIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-10-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ELAGOLIX SODIUM
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ELAGOLIX SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-03-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Voxelotor Adipic Acid Co-Crystal
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VOXELOTOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-03-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
VOXELOTOR FORM-I
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VOXELOTOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-03-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TAFAMIDIS (FORM-4)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
TAFAMIDIS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-03-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ipratropium Bromide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
IPRATROPIUM BROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-05-18
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
ENTACAPONE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ENTACAPONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
EZETIMIBE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
EZETIMIBE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ARIPIPRAZOLE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ARIPIPRAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Voriconazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VORICONAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LINEZOLID
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LINEZOLID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Brinzolamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
BRINZOLAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DEFERASIROX
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DEFERASIROX
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Propofol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PROPOFOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-06-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dabigatran Etexilate Mesylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DABIGATRAN ETEXILATE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-05-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DEUTETRABENAZINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DEUTETRABENAZINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-09-05
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Brinzolamide Sterile
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
BRINZOLAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lurasidone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LURASIDONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-07-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Labetalol Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LABETALOL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-07-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SD-560 d3-Pirfenidone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PIRFENIDONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ciprofloxacin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
CIPROFLOXACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
APIXABAN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
APIXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
RIVAROXABAN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
RIVAROXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Apremilast
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
APREMILAST
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-11-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sugammadex
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
SUGAMMADEX
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-11-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ticagrelor
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
TICAGRELOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-11-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bempedoic Acid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
BEMPEDOIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-04-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
EDARAVONE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
EDARAVONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-09-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TAFAMIDIS MEGLUMINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
TAFAMIDIS MEGLUMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-03-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aripiprazole Monohydrate (Sterile)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ARIPIPRAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MIRABEGRON
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
MIRABEGRON
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-03-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CIPROFLOXACIN HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
CIPROFLOXACIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-03-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
VILOXAZINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VILOXAZINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-03-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
XANOMELINE TARTRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
XANOMELINE TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-03-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Edoxaban Tosylate Monohydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Neuland Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
EDOXABAN TOSYLATE MONOHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-12-19
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
65 total- Bulk Ingredient
Official Source
NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).
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NDC
58032-0002
Nonproprietary Name
ALBUTEROL SULFATE
Labeler
Neuland Laboratories Limited
Dosage Form
POWDER
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