NDC 71335-0024

Nitrofurantion

Nitrofurantion

Nitrofurantion is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Nitrofurantoin.

Product ID71335-0024_eeb12928-61ab-42a0-a1fa-2819b9ffa3cb
NDC71335-0024
Product TypeHuman Prescription Drug
Proprietary NameNitrofurantion
Generic NameNitrofurantion
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2016-04-15
Marketing CategoryANDA /
Application NumberANDA201722
Labeler NameBryant Ranch Prepack
Substance NameNITROFURANTOIN
Active Ingredient Strength100 mg/1
Pharm ClassesNitrofuran Antibacterial [EPC], Nitrofurans [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-0024-1

40 CAPSULE in 1 BOTTLE (71335-0024-1)
Marketing Start Date2022-02-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0024-6 [71335002406]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

NDC 71335-0024-3 [71335002403]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

NDC 71335-0024-8 [71335002408]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

NDC 71335-0024-2 [71335002402]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

NDC 71335-0024-1 [71335002401]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

NDC 71335-0024-5 [71335002405]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

NDC 71335-0024-9 [71335002409]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

NDC 71335-0024-4 [71335002404]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

NDC 71335-0024-7 [71335002407]

Nitrofurantion CAPSULE
Marketing CategoryANDA
Application NumberANDA201722
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2018-01-30

Drug Details

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

NDCBrand NameGeneric Name
50090-5693NitrofurantionNitrofurantion
55700-893NitrofurantionNitrofurantion
57664-231NitrofurantionNitrofurantion
57664-232NitrofurantionNitrofurantion
57664-233NitrofurantionNitrofurantion
61919-024NITROFURANTIONNITROFURANTION
68001-384NitrofurantionNitrofurantion
68001-385NitrofurantionNitrofurantion
68001-386NitrofurantionNitrofurantion
68071-2363NitrofurantionNitrofurantion
68071-2647NitrofurantionNitrofurantion
68071-3134NitrofurantionNitrofurantion
70518-3041NitrofurantionNitrofurantion
70934-413NitrofurantionNitrofurantion
71205-171NitrofurantionNitrofurantion
71335-0024NitrofurantionNitrofurantion
71335-0793NitrofurantionNitrofurantion

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