Micro Labs Limited
NDC Database
Micro Labs Limited
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 25
- Latest Marketing Date 2026-01-01
- Data Source FDA
- First Marketing Date 2010-11-26
Company Overview
Social Profiles
Company Snapshot
NDC Records ( 25 records )
Nonproprietary Name
Celecoxib
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
CELECOXIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-11-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dorzolamide Hydrochloride
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
DORZOLAMIDE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-02-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bepotastine Besilate
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
BEPOTASTINE BESILATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Telmisartan
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TELMISARTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-09-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Olmesartan Medoxomil
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
OLMESARTAN MEDOXOMIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-09-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rasagiline Mesylate
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
RASAGILINE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-09-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bromfenac sodium sesquihydrate
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
BROMFENAC SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-10-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ticagrelor
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TICAGRELOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sodium nitroprusside
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
SODIUM NITROPRUSSIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-04-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Isoproterenol Hydrochloride
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ISOPROTERENOL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-09-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tofacitinib Citrate
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TOFACITINIB CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-06-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Clobazam
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
CLOBAZAM
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
2022-01-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naphazoline Hydrochloride
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
NAPHAZOLINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Methazolamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
METHAZOLAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-03-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Methazolamide
Dosage Form
POWDER
Strength
15 kg/15kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
METHAZOLAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-08-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pirfenidone
Dosage Form
POWDER
Strength
20 kg/20kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PIRFENIDONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-04-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nepafenac
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
NEPAFENAC
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-06-20
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Brimonidine Tartrate
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
BRIMONIDINE TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nitrofurantoin Monohydrate
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
NITROFURANTOIN MONOHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-07-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Anagrelide Hydrochloride
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ANAGRELIDE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-03-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Glimepiride
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
GLIMEPIRIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Cromolyn Sodium
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
CROMOLYN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-06-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pentosan Polysulfate Sodium
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PENTOSAN POLYSULFATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-07-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acrivastine
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ACRIVASTINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-03-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Salcaprozate Sodium
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
Micro Labs Limited
Marketing Category
BULK INGREDIENT
Substance
SALCAPROZATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-06-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
25 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).
Visit FDA NDC DirectoryNDC Record Details Preview
Explore important National Drug Code information available in the records above.
NDC
42571-155
Nonproprietary Name
Celecoxib
Labeler
Micro Labs Limited
Dosage Form
POWDER
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