Benicar
- Product NDC
- 68151-4633
- 11-digit product format
- 681514633
- Labeler code
- 68151
- Product ID
- 68151-4633_ff681737-ed6c-4527-8b1e-05fb087c63b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- NDA021286
- Marketing category
- NDA
- Marketing start
- 2002-04-25
- Marketing end
- 0000-00-00
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-4633-3 | Benicar | 1 in 1 PACKAGE | TABLET, FILM COATED | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-4633 | BENICAR (OLMESARTAN MEDOXOMIL) TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT] | 3 | Legacy NDC, 1 package rows | 20160806_b2d10788-e0e4-4ee8-8c47-d7f7ed44e3d9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-4633-3 | 68151463303 | 1 in 1 PACKAGE | Historical |