NDC 68071-3138 – Carvedilol
Carvedilol 3.125 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3138
Product details
- Brand name
- Carvedilol
- Generic name
- Carvedilol
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077614
- Marketed since
- September 5, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Blocker; beta-Adrenergic Blocker
Active ingredients
- Carvedilol 3.125 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3138-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3138-3) | Mar 1, 2017 |
| 68071-3138-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3138-6) | Mar 1, 2017 |
| 68071-3138-8 | 180 TABLET, FILM COATED in 1 BOTTLE (68071-3138-8) | Mar 1, 2017 |
| 68071-3138-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3138-9) | Mar 1, 2017 |
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