Hydrocodone Bitartrate And Acetaminophen
- Product NDC
- 50090-1517
- 11-digit product format
- 500901517
- Labeler code
- 50090
- Product ID
- 50090-1517_6f581671-9584-4739-9369-5a215e5b6ed0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1517-0 | 50090151700 | 20 TABLET in 1 BOTTLE, PLASTIC (50090-1517-0) | 20 tablet | 2014-12-11 | 0000-00-00 | No | No | Current |
| 50090-1517-7 | 50090151707 | 12 TABLET in 1 BOTTLE, PLASTIC (50090-1517-7) | 12 tablet | 2015-12-04 | 0000-00-00 | No | No | Current |