NDC 71205-276

Famotidine

Famotidine

Famotidine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Proficient Rx Lp. The primary component is Famotidine.

Product ID71205-276_2cee6d8c-271a-42d0-9376-19495177135d
NDC71205-276
Product TypeHuman Prescription Drug
Proprietary NameFamotidine
Generic NameFamotidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2001-04-16
Marketing CategoryANDA / ANDA
Application NumberANDA075511
Labeler NameProficient Rx LP
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 71205-276-10

10 TABLET, FILM COATED in 1 BOTTLE (71205-276-10)
Marketing Start Date2019-05-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71205-276-60 [71205027660]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075511
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-05-01

NDC 71205-276-90 [71205027690]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075511
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-01

NDC 71205-276-20 [71205027620]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075511
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-01

NDC 71205-276-10 [71205027610]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075511
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-01

NDC 71205-276-30 [71205027630]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075511
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-05-01

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE20 mg/1

OpenFDA Data

SPL SET ID:d60bde93-f512-4071-9e4b-1d8318def3bc
Manufacturer
UNII

Pharmacological Class

  • Histamine H2 Receptor Antagonists [MoA]
  • Histamine-2 Receptor Antagonist [EPC]

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
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.