ACETAMINOPHEN AND CODEINE PHOSPHATE
- Product NDC
- 67046-886
- 11-digit product format
- 670460886
- Labeler code
- 67046
- Product ID
- 67046-886_d6953d25-3fc8-e7ec-e053-2995a90a38d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetaminophen and codeine phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- coupler enterprises inc.
- Application
- ANDA040419
- Marketing category
- ANDA
- Marketing start
- 2001-05-31
- 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
- 2023-12-31
- 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 |
|---|
| 67046-886-30 | 67046088630 | 30 TABLET in 1 BLISTER PACK (67046-886-30) | 30 tablet | 2001-05-31 | 0000-00-00 | No | No | Current |