Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 50090-2229
- 11-digit product format
- 500902229
- Labeler code
- 50090
- Product ID
- 50090-2229_0a1cbb27-fac1-45af-a529-735c0ea91fb4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA201013
- Marketing category
- ANDA
- Marketing start
- 2012-04-11
- Marketing end
- 0000-00-00
- Substance
- HYDROCODONE BITARTRATE; ACETAMINOPHEN
- Active strength
- 10 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2229-0 | 50090222900 | 60 TABLET in 1 BOTTLE (50090-2229-0) | 60 tablet | 2019-01-17 | 0000-00-00 | No | No | Current |
| 50090-2229-1 | 50090222901 | 20 TABLET in 1 BOTTLE (50090-2229-1) | 20 tablet | 2015-11-11 | 0000-00-00 | No | No | Current |