NDC 49884-170 – Sodium Phenylbutyrate
Sodium Phenylbutyrate 500 mg/1 · Tablet · Oral
Product NDC49884-170
Product details
- Brand name
- Sodium Phenylbutyrate
- Generic name
- Sodium Phenylbutyrate Tablets, 500 mg
- Labeler
- Par Health USA, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204395
- Marketed since
- April 29, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nitrogen Binding Agent
Active ingredients
- Sodium Phenylbutyrate 500 mg/1
Uses, dosage, side effects and warnings for Sodium phenylbutyrate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 49884-170-04 | 1 BOTTLE in 1 CARTON (49884-170-04) / 250 TABLET in 1 BOTTLE | Apr 29, 2016 |
Other Sodium phenylbutyrate products
- 68462-853 Sodium Phenylbutyrate 500 mg/1 · Tablet · GLENMARK PHARMACEUTICALS INC., USA
- 68475-011 Sodium Phenylbutyrate 500 mg/1 · Tablet · Navinta LLC
- 70710-2180 Sodium Phenylbutyrate 500 mg/1 · Tablet · Zydus Pharmaceuticals USA Inc.
- 49884-006 Sodium Phenylbutyrate .94 g/g · Powder · Par Health USA, LLC