Bufferin Arthritis
- Product NDC
- 55741-000
- 11-digit product format
- 557410000
- Labeler code
- 55741
- Product ID
- 55741-000_9853c3cb-7d1b-d407-446d-363e2c771b4c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspirin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Dr. Reddy's Laboratories Inc.
- Application
- part343
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-07-20
- Marketing end
- 0000-00-00
- Substance
- ASPIRIN
- Active strength
- 325 mg/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 |
|---|
| 55741-000-60 | Bufferin Arthritis | 60 in 1 BOTTLE | TABLET | 60 | | 2 |
| 55741-000-60 | Bufferin Arthritis | 1 in 1 BOX | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55741-000 | BUFFERIN ARTHRITIS (ASPIRIN) TABLET [DR. REDDY'S LABORATORIES INC.] | 2 | Legacy NDC, 2 package rows | 20191211_bf2d3001-a772-ddb1-e17c-3a47b4cbace2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55741-000-60 | 55741000060 | 60 in 1 BOTTLE | Historical |