NDC 16590-126

NDC 16590-126

NDC 16590-126 is a in the category. It is labeled and distributed by .

• Proprietary Name: NDC 16590-126
• Marketing Category: /

Packaging

NDC SPL Data Element Entries

NDC 16590-126-40 [16590012640]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-07-06
• Inactivation Date: 2019-11-13

NDC 16590-126-62 [16590012662]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-11-20
• Marketing End Date: 2012-07-06

NDC 16590-126-90 [16590012690]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-11-20
• Inactivation Date: 2019-11-13

NDC 16590-126-60 [16590012660]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-11-20
• Inactivation Date: 2019-11-13

NDC 16590-126-72 [16590012672]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-11-20
• Inactivation Date: 2019-11-13

NDC 16590-126-30 [16590012630]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-11-20
• Inactivation Date: 2019-11-13

NDC 16590-126-56 [16590012656]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-11-20
• Marketing End Date: 2012-07-06

NDC 16590-126-71 [16590012671]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-11-20
• Inactivation Date: 2019-11-13

NDC 16590-126-50 [16590012650]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-07-06
• Inactivation Date: 2019-11-13

NDC 16590-126-86 [16590012686]

IBUPROFEN TABLET

• Marketing Category: ANDA
• Application Number: ANDA075682
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2008-11-20
• Marketing End Date: 2012-07-06

Drug Details