Acetaminophen
- Product NDC
- 0363-0336
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA076200
- Marketing category
- ANDA
- Substance
- ACETAMINOPHEN
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0363-0336-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0336-01) | 2002-04-30 | 0000-00-00 | No | Current |
| 0363-0336-02 | 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0336-02) | 2019-06-01 | 0000-00-00 | No | Current |
| 0363-0336-24 | 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0336-24) | 2002-04-30 | 0000-00-00 | No | Current |