Acetaminophen and Codeine
- Product NDC
- 51655-808
- 11-digit product format
- 516550808
- Labeler code
- 51655
- Product ID
- 51655-808_d4791ad7-c059-f925-e053-2995a90a9f78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetaminophen and Codeine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA202800
- Marketing category
- ANDA
- Marketing start
- 2016-09-29
- Marketing end
- 0000-00-00
- Substance
- CODEINE PHOSPHATE; ACETAMINOPHEN
- Active strength
- 30 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 |
|---|
| 51655-808-52 | 51655080852 | 30 TABLET in 1 BOTTLE (51655-808-52) | 30 tablet | 2016-09-29 | 0000-00-00 | No | No | Current |
| 51655-808-53 | 51655080853 | 10 TABLET in 1 BOTTLE (51655-808-53) | 10 tablet | 2017-11-30 | 0000-00-00 | No | No | Current |
| 51655-808-54 | 51655080854 | 15 TABLET in 1 BOTTLE (51655-808-54) | 15 tablet | 2016-09-29 | 0000-00-00 | No | No | Current |
| 51655-808-87 | 51655080887 | 6 TABLET in 1 BOTTLE (51655-808-87) | 6 tablet | 2019-06-21 | 0000-00-00 | No | No | Current |