NDC 68788-8880 – Methocarbamol
Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8880
Product details
- Brand name
- Methocarbamol
- Generic name
- Methocarbamol
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203550
- Marketed since
- June 2, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Methocarbamol 500 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8880-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8880-3) | Jun 2, 2025 |
| 68788-8880-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8880-6) | Jun 2, 2025 |
| 68788-8880-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8880-9) | Jun 2, 2025 |
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