NDC 16590-012

NDC 16590-012

NDC 16590-012 is a in the category. It is labeled and distributed by .

• Proprietary Name: NDC 16590-012
• Marketing Category: /

Packaging

NDC SPL Data Element Entries

NDC 16590-012-72 [16590001272]

AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA040218
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1997-09-11
• Inactivation Date: 2019-11-13

NDC 16590-012-90 [16590001290]

AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA040218
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-09-11
• Inactivation Date: 2019-11-13

NDC 16590-012-30 [16590001230]

AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA040218
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-09-11
• Inactivation Date: 2019-11-13

NDC 16590-012-28 [16590001228]

AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA040218
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-09-11
• Inactivation Date: 2019-11-13

NDC 16590-012-60 [16590001260]

AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA040218
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-09-11
• Inactivation Date: 2019-11-13

NDC 16590-012-56 [16590001256]

AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA040218
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1997-09-11
• Inactivation Date: 2019-11-13

NDC 16590-012-82 [16590001282]

AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA040218
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1997-09-11
• Inactivation Date: 2019-11-13

Drug Details