Hydrocodone Bitartrate And Acetaminophen
- Product NDC
- 60760-202
- 11-digit product format
- 607600202
- Labeler code
- 60760
- Product ID
- 60760-202_7cadc747-55a8-8efe-e053-2991aa0a1d8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA040655
- Marketing category
- ANDA
- Marketing start
- 2006-01-19
- Marketing end
- 2019-06-30
- 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