OLMESARTAN MEDOXOMIL
- Product NDC
- 48792-7877
- 11-digit product format
- 487927877
- Labeler code
- 48792
- Product ID
- 48792-7877_8341900b-a242-64cc-e053-2a91aa0a894e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma Co., Ltd.
- Application
- ANDA211049
- Marketing category
- ANDA
- Marketing start
- 2019-03-05
- 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 |
|---|
| 48792-7877-1 | 48792787701 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7877-1) | 2019-03-05 | 0000-00-00 | No | No | Current |