NDC 50989-886

NDC 50989-886

NDC 50989-886 is a in the category. It is labeled and distributed by .

• Proprietary Name: NDC 50989-886
• Marketing Category: /

Packaging

NDC SPL Data Element Entries

NDC 50989-886-16 [50989088616]

Ultigene INJECTION, SOLUTION

• Marketing Category: unapproved drug other
• Product Type: PRESCRIPTION ANIMAL DRUG
• Marketing Start Date: 2019-08-05

NDC 50989-886-17 [50989088617]

Ultigene INJECTION, SOLUTION

• Marketing Category: unapproved drug other
• Product Type: PRESCRIPTION ANIMAL DRUG
• Marketing Start Date: 2019-08-05

Drug Details