National Drug Code (NDC) Database
Apicore Pharmaceuticals Pvt. Ltd.
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NDC:
42973-423
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Nonproprietary Name:
Phentolamine Mesylate
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PHENTOLAMINE MESYLATE
-
Start Marketing Date:
2025-03-14
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
APISTER LIFESCIENCES PRIVATE LIMITED
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NDC:
87621-006
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Nonproprietary Name:
Thymosin Beta-4 Fragment (TB 500) Acetate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 g/100g
-
Substance:
THYMOSIN .BETA.-4
-
Start Marketing Date:
2026-06-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
APL HEALTHCARE LIMITED
-
NDC:
70120-155
-
Nonproprietary Name:
Acetaminophen
-
Dosage Form:
TABLET
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
500 mg/1
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2021-10-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Apotex Corp.
-
NDC:
60505-6420
-
Nonproprietary Name:
Fluticasone Propionate
-
Dosage Form:
SPRAY, METERED
-
Product Type:
HUMAN OTC DRUG
-
Strength:
50 ug/1
-
Substance:
FLUTICASONE PROPIONATE
-
Start Marketing Date:
2025-09-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Apotex Inc.
-
NDC:
49867-0080
-
Nonproprietary Name:
TASIMELTEON
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TASIMELTEON
-
Start Marketing Date:
2017-07-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Apotheca Company
-
NDC:
57520-1706
-
Nonproprietary Name:
Aralia Quinquefolia, Arnica Montana, Avena Sativa, Baryta Carbonica, Carduus Marianus, Hepar Suis, Medulla Ossis Suis, Pancreas Suis, Phosphoricum Acidum, Pituitarum Posterium (Bovine), Thuja Occidentalis
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
4; 4; 6; 30; 12; 4; 4; 6; 6; 6; 30 mL; mL; mL; mL; mL; mL; mL; mL; mL; mL; mL
-
Substance:
AMERICAN GINSENG; ARNICA MONTANA WHOLE; AVENA SATIVA FLOWERING TOP; BARIUM CARBONATE; BOS TAURUS PITUITARY GLAND, POSTERIOR; MILK THISTLE; PHOSPHORIC ACID; PORK LIVER; SUS SCROFA BONE MARROW; SUS SCROFA PANCREAS; THUJA OCCIDENTALIS LEAFY TWIG
-
Start Marketing Date:
2026-03-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Apothecon Pharmaceuticals Pvt Ltd
-
NDC:
76339-517
-
Nonproprietary Name:
Glycerol Phenylbutyrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
4.999 kg/4.999kg
-
Substance:
GLYCEROL PHENYLBUTYRATE
-
Start Marketing Date:
2025-11-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Applechem, Inc.
-
NDC:
83396-0001
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.7 kg/kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2013-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Applied Laboratories, Inc.
-
NDC:
72751-2302
-
Nonproprietary Name:
Cetylpyridinium Chloride
-
Dosage Form:
MOUTHWASH
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 mg/.001L
-
Substance:
CETYLPYRIDINIUM CHLORIDE
-
Start Marketing Date:
2018-11-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Aptuit (Oxford) Ltd
-
NDC:
71924-0064
-
Nonproprietary Name:
MAVORIXAFOR
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MAVORIXAFOR
-
Start Marketing Date:
2024-04-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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