14803-135-00
- Product NDC
- 14803-135
- Requested package NDC
- 14803-135-00
- 11-digit product format
- 148030135
- Labeler code
- 14803
- Product ID
- 14803-135_4ab35bfe-1982-35a0-e063-6294a90aadcf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen aspirin and caffeine
- Dosage form
- TABLET
- Marketing category
- DRUG FOR FURTHER PROCESSING
- Marketing start
- 2024-01-30
- Substance
- ACETAMINOPHEN; ASPIRIN; CAFFEINE
- Active strength
- 250 mg/1; 65 mg/1
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- No
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 250 mg/1 |
| ASPIRIN | 250 mg/1 |
| CAFFEINE | 65 mg/1 |
DailyMed Product Concepts#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Status |
|---|
| 14803-135-00 | 14803013500 | 30000 TABLET in 1 BOTTLE (14803-135-00) | 30000 tablet | 30-JAN-24 | Current |