Redicare Ibuprofen
- Product NDC
- 71105-750
- 11-digit product format
- 711050750
- Labeler code
- 71105
- Product ID
- 71105-750_c62a04fc-686f-112d-e053-2a95a90ae61e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen 200mg
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Redicare LLC
- Application
- ANDA079129
- Marketing category
- ANDA
- Marketing start
- 2017-02-01
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 1/2001
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71105-750-68 | Redicare Ibuprofen | 1 in 1 BOX | TABLET, FILM COATED | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71105-750 | REDICARE IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [REDICARE LLC] | 3 | Legacy NDC, 1 package rows | 20210703_45eb33f0-71e2-11d5-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71105-750-68 | 71105075068 | 1 TABLET, FILM COATED in 1 BOX (71105-750-68) | 2017-02-01 | 0000-00-00 | No | No | Current |