NDC 68071-3859 – Methocarbamol
Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3859
Product details
- Brand name
- Methocarbamol
- Generic name
- Methocarbamol
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213967
- Marketed since
- August 12, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Methocarbamol 750 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3859-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-3859-2) | Jun 4, 2025 |
| 68071-3859-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3) | Dec 24, 2025 |
| 68071-3859-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3859-9) | Jan 14, 2025 |
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