ACETAMINOPHEN AND CODEINE
- Product NDC
- 51655-802
- 11-digit product format
- 516550802
- Labeler code
- 51655
- Product ID
- 51655-802_cea4b272-8e61-452d-9ea3-ceff10a203dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Codeine Phosphate and APAP
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals, LLC
- Application
- ANDA040779
- Marketing category
- ANDA
- Marketing start
- 2014-07-18
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-802 | ACETAMINOPHEN AND CODEINE (CODEINE PHOSPHATE AND APAP) TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 3 | Legacy NDC | 20140819_4ad84de7-80c6-41dd-875c-3dd33d19ab45.zip |