Sunmark migraine relief
- Product NDC
- 49348-506
- 11-digit product format
- 493480506
- Labeler code
- 49348
- Product ID
- 49348-506_27fbbd48-0bb6-4580-b2be-d930e7b9d027
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Aspirin, Caffeine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA075794
- Marketing category
- ANDA
- Marketing start
- 2003-08-18
- Marketing end
- 2022-06-30
- Substance
- ACETAMINOPHEN; ASPIRIN; CAFFEINE
- Active strength
- 250 mg/1; mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49348-506-10 | 49348050610 | 1 BOTTLE in 1 CARTON (49348-506-10) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2003-08-18 | 2022-06-30 | No | No | Current |