Ibuprofen
- Product NDC
- 0363-0392
- 11-digit product format
- 003630392
- Labeler code
- 0363
- Product ID
- 0363-0392_2dfa1c2c-66e3-4cea-8dc1-7cf8a58de620
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA075139
- Marketing category
- ANDA
- Marketing start
- 1999-03-01
- Marketing end
- 2023-07-12
- 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 |
|---|
| 0363-0392-12 | 00363039212 | 1 BOTTLE in 1 CARTON (0363-0392-12) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1999-03-01 | 2023-07-12 | No | No | Current |
| 0363-0392-14 | 00363039214 | 500 TABLET, FILM COATED in 1 BOTTLE (0363-0392-14) | | 1999-03-01 | 2023-07-12 | No | No | Current |
| 0363-0392-15 | 00363039215 | 1 BOTTLE in 1 CARTON (0363-0392-15) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1999-03-01 | 2023-07-12 | No | No | Current |
| 0363-0392-16 | 00363039216 | 1000 TABLET, FILM COATED in 1 BOTTLE (0363-0392-16) | | 1999-03-01 | 2023-07-12 | No | No | Current |
| 0363-0392-17 | 00363039217 | 300 TABLET, FILM COATED in 1 BOTTLE (0363-0392-17) | | 1999-03-01 | 2023-07-12 | No | No | Current |