IBUPROFEN
- Product NDC
- 67060-002
- 11-digit product format
- 670600002
- Labeler code
- 67060
- Product ID
- 67060-002_f29f20ae-0327-4038-b377-8662689256bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN 200MG
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ADVANCED FIRST AID, INC.
- Application
- ANDA091239
- Marketing category
- ANDA
- Marketing start
- 2019-03-20
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 1/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 67060-002-67 | IBUPROFEN | 2 in 1 PACKET | TABLET, FILM COATED | 2 | | 1 |
| 67060-002-67 | IBUPROFEN | 250 in 1 CARTON | TABLET, FILM COATED | 250 | | 1 |
| 67060-002-68 | IBUPROFEN | 2 in 1 PACKET | TABLET, FILM COATED | 2 | | 1 |
| 67060-002-68 | IBUPROFEN | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67060-002 | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | Legacy NDC, 4 package rows | 20190403_2f063e11-9415-4ad4-b533-206384eb9840.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67060-002-67 | 67060000267 | 250 PACKET in 1 CARTON (67060-002-67) > 2 TABLET, FILM COATED in 1 PACKET | 250 packet | 2019-03-20 | 0000-00-00 | No | No | Current |
| 67060-002-68 | 67060000268 | 100 PACKET in 1 CARTON (67060-002-68) > 2 TABLET, FILM COATED in 1 PACKET | 100 packet | 2019-03-20 | 0000-00-00 | No | No | Current |