Norco
- Product NDC
- 0023-6022
- 11-digit product format
- 000236022
- Labeler code
- 0023
- Product ID
- 0023-6022_5ceeb45a-154d-4835-88f2-73bafcc10735
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Allergan, Inc.
- Application
- ANDA040148
- Marketing category
- ANDA
- Marketing start
- 2013-03-12
- Marketing end
- 2021-11-30
- 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
- 0000-00-00
- 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 |
|---|
| 0023-6022-01 | 00023602201 | 100 TABLET in 1 BOTTLE, PLASTIC (0023-6022-01) | 100 tablet | 2013-03-12 | 2021-11-30 | No | No | Current |
| 0023-6022-05 | 00023602205 | 500 TABLET in 1 BOTTLE, PLASTIC (0023-6022-05) | 500 tablet | 2013-03-12 | 2021-11-30 | No | No | Current |