Acetaminophen and Codeine
- Product NDC
- 66267-759
- 11-digit product format
- 662670759
- Labeler code
- 66267
- Product ID
- 66267-759_b8a7caa7-bfb5-7fb6-e053-2a95a90af5de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetaminophen and Codeine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040779
- Marketing category
- ANDA
- Marketing start
- 2008-05-29
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66267-759-02 | 66267075902 | 12 TABLET in 1 BOTTLE (66267-759-02) | 12 tablet | 2018-01-22 | 0000-00-00 | No | No | Current |
| 66267-759-04 | 66267075904 | 4 TABLET in 1 BOTTLE (66267-759-04) | 4 tablet | 2018-01-22 | 0000-00-00 | No | No | Current |
| 66267-759-06 | 66267075906 | 6 TABLET in 1 BOTTLE (66267-759-06) | 6 tablet | 2018-01-22 | 0000-00-00 | No | No | Current |