Acetaminophen and Codeine Phosphate
- Product NDC
- 68071-4668
- 11-digit product format
- 680714668
- Labeler code
- 68071
- Product ID
- 68071-4668_bb8b684c-faee-260c-e053-2a95a90a4187
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetaminophen and Codeine Phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202800
- Marketing category
- ANDA
- Marketing start
- 2013-04-15
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; CODEINE PHOSPHATE
- Active strength
- 300 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-4668-6 | 68071466806 | 6 TABLET in 1 BOTTLE (68071-4668-6) | 6 tablet | 2018-12-17 | 0000-00-00 | No | No | Current |