Vicodin
- Product NDC
- 0074-3041
- 11-digit product format
- 000743041
- Labeler code
- 0074
- Product ID
- 0074-3041_7d64905a-8c65-cf23-e053-2a91aa0a5c9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AbbVie Inc.
- Application
- ANDA040658
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- Marketing end
- 2019-09-29
- Substance
- HYDROCODONE BITARTRATE; ACETAMINOPHEN
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Opioid Agonist [EPC],Opioid Agonists [MoA]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record