Ibuprofen
- Product NDC
- 0536-1089
- 11-digit product format
- 005361089
- Labeler code
- 0536
- Product ID
- 0536-1089_22bd8b8b-a455-4102-81d0-7822c09998f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rugby Laboratories
- Application
- ANDA075010
- Marketing category
- ANDA
- Marketing start
- 1988-05-24
- Marketing end
- 2022-11-06
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0536-1089-01 | 00536108901 | 1 BOTTLE in 1 CARTON (0536-1089-01) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1988-05-24 | 2022-11-06 | No | No | Current |