Walgreen
- Product NDC
- 0363-9125
- 11-digit product format
- 003639125
- Labeler code
- 0363
- Product ID
- 0363-9125_446a1072-4099-0951-e063-6394a90a9e5d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth Subsalicylate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- WALGREEN CO.
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-05-14
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 mg/1
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Walgreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 262 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308760 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-9125-40 | Walgreen | 40 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 40 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-9125 | WALGREEN (BISMUTH SUBSALICYLATE) TABLET, FILM COATED [WALGREEN CO.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241110_73231515-840f-4086-86da-4b815d664c13.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-9125-40 | 00363912540 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-9125-40) | 2019-05-14 | 0000-00-00 | No | No | Current |