Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 60760-218
- 11-digit product format
- 607600218
- Labeler code
- 60760
- Product ID
- 60760-218_98328c07-6888-74a6-e053-2a95a90aa639
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA201013
- Marketing category
- ANDA
- Marketing start
- 2012-04-11
- Marketing end
- 2020-07-31
- 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