rx act ibuprofen
- Product NDC
- 37808-897
- 11-digit product format
- 378080897
- Labeler code
- 37808
- Product ID
- 37808-897_cec6ab78-18da-40cd-b32d-a8f86bee870d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA074937
- Marketing category
- ANDA
- Marketing start
- 1999-01-06
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 100 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-897 | RX ACT IBUPROFEN CHILDRENS (IBUPROFEN) SUSPENSION [H E B] | 4 | Legacy NDC | 20191205_dbcf47cc-4dc7-4110-b64d-4e1d52e05d47.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-897-26 | 37808089726 | 1 BOTTLE in 1 CARTON (37808-897-26) > 120 mL in 1 BOTTLE | 1 bottle | 1999-01-06 | 0000-00-00 | No | No | Current |