NDC 16590-116

NDC 16590-116

NDC 16590-116 is a in the category. It is labeled and distributed by .

• Proprietary Name: NDC 16590-116
• Marketing Category: /

Packaging

NDC SPL Data Element Entries

NDC 16590-116-90 [16590011690]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA040094
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1995-09-29
• Inactivation Date: 2019-11-13

NDC 16590-116-40 [16590011640]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA040094
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1995-09-29
• Inactivation Date: 2019-11-13

NDC 16590-116-20 [16590011620]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA040094
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1995-09-29
• Inactivation Date: 2019-11-13

NDC 16590-116-72 [16590011672]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA040094
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1995-09-29
• Inactivation Date: 2019-11-13

NDC 16590-116-60 [16590011660]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA040094
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1995-09-29
• Inactivation Date: 2019-11-13

NDC 16590-116-30 [16590011630]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA040094
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1995-09-29
• Inactivation Date: 2019-11-13

Drug Details