GEWORIN
- Product NDC
- 72689-0019
- 11-digit product format
- 726890019
- Labeler code
- 72689
- Product ID
- 72689-0019_7cb69565-a850-ec6e-e053-2991aa0a59e6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Caffeine Anhydrous, Isopropylantipyrine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- OASIS TRADING
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-11-20
- Marketing end
- 0000-00-00
- Substance
- PROPYPHENAZONE; ACETAMINOPHEN; CAFFEINE
- Active strength
- 150 mg/1; mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 72689-0019-1 | GEWORIN | 10 in 1 BLISTER PACK | TABLET | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72689-0019 | GEWORIN (ACETAMINOPHEN, CAFFEINE ANHYDROUS, ISOPROPYLANTIPYRINE) TABLET [OASIS TRADING] | 1 | Legacy NDC, 1 package rows | 20181211_7cb69565-a84f-ec6e-e053-2991aa0a59e6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 72689-0019-1 | 72689001901 | 10 in 1 BLISTER PACK | Historical |