National Drug Code (NDC) Database
Avra Laboratories Pvt. Ltd.
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NDC:
70772-0005
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Nonproprietary Name:
S-8-Ethyl-8-hydroxy-2,3,5,8-tetrahydro-6-oxa-3-aza-cyclopenta naphthalene-1,4,7-trione
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
4-ETHYL-4-HYDROXY-7,8-DIHYDRO-1H-PYRANO(3,4-F)INDOLIZINE-3,6,10(4H)-TRIONE, (S)-
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Start Marketing Date:
2024-05-01
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
AX Pharmaceutical Corp
-
NDC:
73377-358
-
Nonproprietary Name:
Bupropion HCl
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
BUPROPION HYDROCHLORIDE
-
Start Marketing Date:
2026-06-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
AX Pharmaceutical Corp.
-
NDC:
73377-324
-
Nonproprietary Name:
Oxymetazoline HCl
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
OXYMETAZOLINE HYDROCHLORIDE
-
Start Marketing Date:
2025-06-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Azico Biophore India Private Limited
-
NDC:
69575-4059
-
Nonproprietary Name:
Selenious acid
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
SELENIOUS ACID
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Start Marketing Date:
2021-12-16
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Azurity Pharmaceutcials, Inc.
-
NDC:
65628-080
-
Nonproprietary Name:
Lansoprazole
-
Dosage Form:
KIT
-
Product Type:
BULK INGREDIENT
-
Strength:
-
Substance:
-
Start Marketing Date:
2011-12-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Azurity Pharmaceuticals, Inc.
-
NDC:
65628-202
-
Nonproprietary Name:
Metronidazole Benzoate
-
Dosage Form:
KIT
-
Product Type:
BULK INGREDIENT
-
Strength:
-
Substance:
-
Start Marketing Date:
2016-09-26
-
End Marketing Date:
2027-01-07
-
DEA Schedule:
-
Certified Through:
0000-00-00
B.V KATWIJK CHEMIE
-
NDC:
17349-0020
-
Nonproprietary Name:
Sodium Valproate Powder
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
VALPROATE SODIUM
-
Start Marketing Date:
2005-01-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
B.V. KATWIJK CHEMIE
-
NDC:
17349-0023
-
Nonproprietary Name:
DEFERIPRONE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
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Strength:
25 kg/25kg
-
Substance:
DEFERIPRONE
-
Start Marketing Date:
2018-03-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Bajaj Healthcare Ltd
-
NDC:
84855-015
-
Nonproprietary Name:
Ascorbic Acid
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ASCORBIC ACID
-
Start Marketing Date:
2024-02-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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