Pain Relief - Ibuprofen 200 mg
- Product NDC
- 71679-111
- 11-digit product format
- 716790111
- Labeler code
- 71679
- Product ID
- 71679-111_d60a6772-4667-6b30-e053-2995a90a7516
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Health Pharma USA LLC
- Application
- ANDA079174
- Marketing category
- ANDA
- Marketing start
- 2022-01-01
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pain Relief - Ibuprofen 200 mg
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 310965 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71679-111-05 | Pain Relief - Ibuprofen 200 mg | 500 in 1 BOTTLE | TABLET, COATED | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71679-111 | PAIN RELIEF - IBUPROFEN 200 MG (IBUPROFEN) TABLET, COATED [HEALTH PHARMA USA LLC] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220121_d60a6a11-8c06-cede-e053-2a95a90af7f9.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 |
|---|
| 71679-111-05 | 71679011105 | 500 TABLET, COATED in 1 BOTTLE (71679-111-05) | 2022-01-01 | 0000-00-00 | No | No | Current |