Acetaminophen and Codeine Phosphate
- Product NDC
- 50090-1934
- 11-digit product format
- 500901934
- Labeler code
- 50090
- Product ID
- 50090-1934_cb34aa1a-345c-427b-8e8f-22f3d519e621
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetaminophen and Codeine Phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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 |
|---|
| 50090-1934-0 | 50090193400 | 40 TABLET in 1 BOTTLE (50090-1934-0) | 40 tablet | 2015-07-16 | 0000-00-00 | No | No | Current |
| 50090-1934-1 | 50090193401 | 16 TABLET in 1 BOTTLE (50090-1934-1) | 16 tablet | 2015-07-16 | 0000-00-00 | No | No | Current |
| 50090-1934-6 | 50090193406 | 60 TABLET in 1 BOTTLE (50090-1934-6) | 60 tablet | 2015-07-16 | 0000-00-00 | No | No | Current |