Valsartan
- Product NDC
- 50268-786
- 11-digit product format
- 502680786
- Labeler code
- 50268
- Product ID
- 50268-786_d5e0cf6a-8e97-6810-e053-2995a90a656c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA203311
- Marketing category
- ANDA
- Marketing start
- 2016-06-29
- Marketing end
- 0000-00-00
- Substance
- VALSARTAN
- Active strength
- 320 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-786-13 | 50268078613 | 30 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (50268-786-13) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-786-11) | 30 blister pack | 2016-06-29 | 0000-00-00 | No | No | Current |