Excedrin
- Product NDC
- 0067-8202
- 11-digit product format
- 000678202
- Labeler code
- 0067
- Product ID
- 0067-8202_93bc5c3b-f2e7-41e3-aa3a-0a181c3477cf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Aspirin (NSAID), and Caffeine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-09
- Substance
- ACETAMINOPHEN; ASPIRIN; CAFFEINE
- Active strength
- 250; 250; 65 mg/1; mg/1; mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Excedrin
- Brand name suffix
- Extra Strength Pain Reliever
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 250 mg/1 |
| ASPIRIN | 250 mg/1 |
| CAFFEINE | 65 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D, R16CO5Y76E, 3G6A5W338E |
| Rxcui | 209468, 308297 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0067-8202-03 | ExcedrinExtra Strength Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 3 |
| 0067-8202-03 | ExcedrinExtra Strength Pain Reliever | 300 in 1 BOTTLE | TABLET, FILM COATED | 300 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0067-8202 | EXCEDRIN EXTRA STRENGTH PAIN RELIEVER (ACETAMINOPHEN, ASPIRIN (NSAID), AND CAFFEINE) TABLET, FILM COATED [HALEON US HOLDINGS LLC] | 3 | Current NDC, Legacy NDC, 2 package rows | 20240316_691b754c-bafc-47e2-a322-cf56245c01f6.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 |
|---|
| 0067-8202-03 | 00067820203 | 1 BOTTLE in 1 CARTON (0067-8202-03) / 300 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-03-09 | 0000-00-00 | No | No | Current |