Olmesartan Medoxomil
- Product NDC
- 0378-7012
- 11-digit product format
- 003787012
- Labeler code
- 0378
- Product ID
- 0378-7012_1ddd9739-cbdc-4147-953e-3706f634f0a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA078276
- Marketing category
- ANDA
- Marketing start
- 2016-10-26
- 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
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0378-7012-93 | 00378701293 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7012-93) | 2016-10-26 | 0000-00-00 | No | No | Current |