Ibuprofen
- Product NDC
- 36800-969
- 11-digit product format
- 368000969
- Labeler code
- 36800
- Product ID
- 36800-969_d0c81334-185c-26ce-e053-2995a90a0923
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- TopCare
- Application
- ANDA079174
- Marketing category
- ANDA
- Marketing start
- 2019-10-07
- Marketing end
- 2022-05-31
- Substance
- IBUPROFEN
- Active strength
- 200 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 |
|---|
| 36800-969-07 | 36800096907 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (36800-969-07) | 2019-10-07 | 0000-00-00 | No | No | Current |
| 36800-969-20 | 36800096920 | 200 TABLET, COATED in 1 BOTTLE, PLASTIC (36800-969-20) | 2019-10-07 | 0000-00-00 | No | No | Current |