Caffeine
- Product NDC
- 69842-509
- 11-digit product format
- 698420509
- Labeler code
- 69842
- Product ID
- 69842-509_4b987a78-00ba-74d6-e063-6394a90abcde
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Caffeine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CVS Pharmacy, Inc.
- Application
- M011
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-06-22
- Substance
- CAFFEINE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Caffeine
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAFFEINE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3G6A5W338E |
| Rxcui | 198520 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69842-509 | CAFFEINE TABLET [CVS PHARMACY, INC.] | 3 | Current NDC, Legacy NDC, 6 package rows | 20240509_6d9b3926-7198-5e00-e053-2a91aa0a9580.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 |
|---|
| 69842-509-10 | 69842050910 | 5 BLISTER PACK in 1 CARTON (69842-509-10) / 8 TABLET in 1 BLISTER PACK | 5 blister pack | 2018-06-22 | 0000-00-00 | No | No | Current |
| 69842-509-21 | 69842050921 | 2 BLISTER PACK in 1 CARTON (69842-509-21) > 8 TABLET in 1 BLISTER PACK | 2 blister pack | 2018-06-22 | 0000-00-00 | No | No | Current |
| 69842-509-31 | 69842050931 | 1 BOTTLE in 1 CARTON (69842-509-31) / 80 TABLET in 1 BOTTLE | 1 bottle | 2018-06-22 | 0000-00-00 | No | No | Current |