NDC 50111-308

NDC 50111-308

NDC 50111-308 is a in the category. It is labeled and distributed by .

• Proprietary Name: NDC 50111-308
• Marketing Category: /

Packaging

NDC SPL Data Element Entries

NDC 50111-308-02 [50111030802]

Hydroxyzine Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA088618
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1990-09-30
• Marketing End Date: 2013-03-31

NDC 50111-308-01 [50111030801]

Hydroxyzine Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA088618
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1990-09-30
• Marketing End Date: 2013-03-31

NDC 50111-308-03 [50111030803]

Hydroxyzine Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA088618
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1990-09-30
• Marketing End Date: 2013-03-31

Drug Details