NDC 71335-1072

Metformin HCl

Metformin Hcl

Metformin HCl is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Metformin Hydrochloride.

Product ID71335-1072_ce0f2d32-bacf-4573-b074-58707f9e4b59
NDC71335-1072
Product TypeHuman Prescription Drug
Proprietary NameMetformin HCl
Generic NameMetformin Hcl
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-02-06
Marketing CategoryANDA / ANDA
Application NumberANDA090564
Labeler NameBryant Ranch Prepack
Substance NameMETFORMIN HYDROCHLORIDE
Active Ingredient Strength500 mg/1
Pharm ClassesBiguanide [EPC],Biguanides [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71335-1072-0

25 TABLET in 1 BOTTLE (71335-1072-0)
Marketing Start Date2019-02-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1072-2 [71335107202]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-1 [71335107201]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-5 [71335107205]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-0 [71335107200]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-6 [71335107206]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-8 [71335107208]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-4 [71335107204]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-3 [71335107203]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-9 [71335107209]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

NDC 71335-1072-7 [71335107207]

Metformin HCl TABLET
Marketing CategoryANDA
Application NumberANDA090564
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-01

Drug Details

Active Ingredients

IngredientStrength
METFORMIN HYDROCHLORIDE500 mg/1

OpenFDA Data

SPL SET ID:4bdd2faa-2125-4139-b958-196393e31b7e
Manufacturer
UNII

Pharmacological Class

  • Biguanide [EPC]
  • Biguanides [CS]
  • Biguanide [EPC]
  • Biguanides [CS]

NDC Crossover Matching brand name "Metformin HCl" or generic name "Metformin Hcl"

NDCBrand NameGeneric Name
42708-009Metformin HClMetformin HCl
42708-018Metformin HClMetformin HCl
49483-620METFORMIN HCLMETFORMIN HCL
49483-621METFORMIN HCLMETFORMIN HCL
49483-622METFORMIN HCLMETFORMIN HCL
50090-3050Metformin HClMetformin HCl
50090-3064Metformin HClMetformin HCl
50090-3579Metformin HClMetformin HCl
50090-4891Metformin HClMetformin HCl
50090-4892Metformin HClMetformin HCl
53002-2251Metformin HClMetformin HCl
53002-2445Metformin HClMetformin HCl
55700-666Metformin HClMetformin HCl
55700-669Metformin HClMetformin HCl
55700-924Metformin HClMetformin HCl
63629-7694Metformin HClMetformin HCl
67296-1604Metformin HClMetformin HCl
67877-561Metformin HClMetformin HCl
67877-562Metformin HClMetformin HCl
67877-563Metformin HClMetformin HCl
68071-4420Metformin HClMetformin HCl
70882-124Metformin HClMetformin HCl
70934-135Metformin HClMetformin HCl
70934-212Metformin HClMetformin HCl
71335-1072Metformin HClMetformin HCl

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