Zamicet
- Product NDC
- 0121-1542
- 11-digit product format
- 001211542
- Labeler code
- 0121
- Product ID
- 0121-1542_2872e73b-2895-4319-8c65-2ec29c17d0ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCODONE BITARTRATE and ACETAMINOPHEN
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- ANDA040834
- Marketing category
- ANDA
- Marketing start
- 2008-08-18
- Marketing end
- 0000-00-00
- Substance
- HYDROCODONE BITARTRATE; ACETAMINOPHEN
- Active strength
- 5 mg/7.5mL; mg/7.5mL
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0121-1542-40 | 00121154240 | 4 TRAY in 1 CASE (0121-1542-40) > 10 CUP, UNIT-DOSE in 1 TRAY > 7.5 mL in 1 CUP, UNIT-DOSE (0121-1542-07) | 4 tray | 2008-08-18 | 0000-00-00 | No | No | Current |