Acetaminophen
- Product NDC
- 0363-0334
- 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 |
|---|
| 0363-0334-22 | 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0334-22) | 2002-04-30 | 0000-00-00 | No | Current |
| 0363-0334-55 | 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0334-55) | 2002-04-30 | 0000-00-00 | No | Current |