Hydrocodone Bitartrate And Acetaminophen
- Product NDC
- 55700-261
- 11-digit product format
- 557000261
- Labeler code
- 55700
- Product ID
- 55700-261_ca5c745a-2a5b-43b8-acc3-856f2cbf5df8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA040655
- Marketing category
- ANDA
- Marketing start
- 2006-01-19
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record