dye-free pain relief
- Product NDC
- 69452-302
- 11-digit product format
- 694520302
- Labeler code
- 69452
- Product ID
- 69452-302_3bcb3a5c-d8b2-33eb-e063-6394a90a67ec
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Bionpharma Inc.
- Application
- ANDA078682
- Marketing category
- ANDA
- Marketing start
- 2021-03-05
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1201
- 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
- dye-free pain relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 200 mg/1201 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 310964 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69452-302-25 | dye-free pain relief | 180 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 180 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69452-302 | DYE-FREE PAIN RELIEF (IBUPROFEN) CAPSULE, LIQUID FILLED [BIONPHARMA INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20221221_c46c9c36-8844-7b50-e053-2a95a90aa0e9.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 |
|---|
| 69452-302-25 | 69452030225 | 180 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-302-25) | 2021-03-05 | 0000-00-00 | No | No | Current |