NDC 54868-1082

NDC 54868-1082

NDC 54868-1082 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 54868-1082
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 54868-1082-0 [54868108200]

Prochlorperazine Maleate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040101
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-01-07
Inactivation Date2019-09-24

NDC 54868-1082-5 [54868108205]

Prochlorperazine Maleate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040101
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-01-07
Inactivation Date2019-09-24

NDC 54868-1082-6 [54868108206]

Prochlorperazine Maleate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040101
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-01-07
Inactivation Date2019-09-24

NDC 54868-1082-4 [54868108204]

Prochlorperazine Maleate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040101
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-01-07
Inactivation Date2019-09-24

NDC 54868-1082-1 [54868108201]

Prochlorperazine Maleate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040101
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-01-07
Inactivation Date2019-09-24

NDC 54868-1082-3 [54868108203]

Prochlorperazine Maleate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040101
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-01-07
Inactivation Date2019-09-24

NDC 54868-1082-2 [54868108202]

Prochlorperazine Maleate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040101
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-01-07
Inactivation Date2019-09-24

Drug Details

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