NDC 68462-447 – Sevelamer hydrochloride
Sevelamer Hydrochloride 800 mg/1 · Tablet, Film Coated · Parenteral
Product NDC68462-447
Product details
- Brand name
- Sevelamer hydrochloride
- Generic name
- Sevelamer hydrochloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Parenteral
- Marketing category
- ANDA · ANDA204724
- Marketed since
- February 8, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phosphate Binder
Active ingredients
- Sevelamer Hydrochloride 800 mg/1
Uses, dosage, side effects and warnings for Sevelamer Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68462-447-18 | 180 TABLET, FILM COATED in 1 BOTTLE (68462-447-18) | Feb 8, 2019 |
| 68462-447-30 | 30 TABLET, FILM COATED in 1 BOTTLE (68462-447-30) | Feb 8, 2019 |
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