NDC 65862-859

Famotidine

Famotidine

Famotidine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Famotidine.

Product ID65862-859_39b63a6c-c329-48d4-bc79-db802f8b8b6b
NDC65862-859
Product TypeHuman Prescription Drug
Proprietary NameFamotidine
Generic NameFamotidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2015-12-22
Marketing CategoryANDA / DRUG FOR FURTHER PROCESSING
Application NumberANDA206530
Labeler NameAurobindo Pharma Limited
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 65862-859-01

100 TABLET, FILM COATED in 1 BOTTLE (65862-859-01)
Marketing Start Date2015-12-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65862-859-10 [65862085910]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206530
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-12-22

NDC 65862-859-05 [65862085905]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206530
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-12-22

NDC 65862-859-99 [65862085999]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206530
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-12-22

NDC 65862-859-30 [65862085930]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206530
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-12-22

NDC 65862-859-01 [65862085901]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206530
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-12-22

NDC 65862-859-78 [65862085978]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206530
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-12-22

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE20 mg/1

Medicade Reported Pricing

65862085999 FAMOTIDINE 20 MG TABLET

Pricing Unit: EA | Drug Type:

65862085901 FAMOTIDINE 20 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Famotidine" or generic name "Famotidine"

NDCBrand NameGeneric Name
0093-2748FamotidineFamotidine
0172-5728FamotidineFamotidine
0172-5729FamotidineFamotidine
0338-5197FamotidineFamotidine
0363-0036FamotidineFamotidine
0363-1899FamotidineFamotidine
68001-240FamotidineFamotidine
68001-241FamotidineFamotidine
68071-1879FamotidineFamotidine
68071-3181FamotidineFamotidine
68071-1941FamotidineFamotidine
68071-3305FamotidineFamotidine
68071-4197FamotidineFamotidine
68071-3201FamotidineFamotidine
68151-0184FamotidineFamotidine
68151-0185FamotidineFamotidine
68180-150FamotidineFamotidine
68210-0007FAMOTIDINEFAMOTIDINE
68382-444FamotidineFamotidine
68645-140FamotidineFamotidine
68645-141FamotidineFamotidine
68788-6859FamotidineFamotidine
68788-6399FamotidineFamotidine
68788-9217FamotidineFamotidine
68788-7191FamotidineFamotidine
68788-9549FamotidineFamotidine
68788-9220FamotidineFamotidine
68788-9779FamotidineFamotidine
70253-128FamotidineFamotidine
70518-0460FamotidineFamotidine
70518-0461FamotidineFamotidine
70518-0163FamotidineFamotidine
70518-1415FamotidineFamotidine
70518-1341FamotidineFamotidine
70518-1001FamotidineFamotidine
70518-1089FamotidineFamotidine
70518-1877FamotidineFamotidine
71335-0409FamotidineFamotidine
0615-4582FamotidineFamotidine
71335-0370FamotidineFamotidine
0615-4594FamotidineFamotidine
72036-026FamotidineFamotidine
0641-6023FamotidineFamotidine
0641-6022FamotidineFamotidine
0641-6021FamotidineFamotidine
10544-481FamotidineFamotidine
12634-967FamotidineFamotidine
15127-370FamotidineFamotidine
33261-185FamotidineFamotidine
33261-562FamotidineFamotidine
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