Acetaminophen
- Product NDC
- 41520-333
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Sales Company
- Application
- ANDA076200
- Marketing category
- ANDA
- Substance
- ACETAMINOPHEN
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
No records found.
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Drug Facts | American Sales Company | Ranbaxy Pharmaceuticals Inc. | Ohm Laboratories Inc. | 2013-01-17 | HUMAN OTC DRUG LABEL | 1 |