NDC 70022-001

NDC 70022-001

NDC 70022-001 is a in the category. It is labeled and distributed by .

• Proprietary Name: NDC 70022-001
• Marketing Category: /

Packaging

NDC SPL Data Element Entries

NDC 70022-001-10 [70022000110]

buprenorphine INJECTION, SOLUTION

• Marketing Category: unapproved drug other
• Product Type: ANIMAL COMPOUNDED DRUG
• Marketing Start Date: 2015-09-11

Drug Details