Acetaminophen
- Product NDC
- 63868-591
- 11-digit product format
- 638680591
- Labeler code
- 63868
- Product ID
- 63868-591_d010a67b-87df-823b-e053-2995a90a6760
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION INC
- Application
- ANDA211544
- Marketing category
- ANDA
- Marketing start
- 2019-10-22
- Marketing end
- 2022-06-30
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-591-02 | 63868059102 | 225 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63868-591-02) | 2019-10-22 | 0000-00-00 | No | No | Current |