NDC 85509-1341 – Methocarbamol
Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral
Product NDC85509-1341
Product details
- Brand name
- Methocarbamol
- Generic name
- Methocarbamol
- Labeler
- PHOENIX RX LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213967
- Marketed since
- August 12, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Methocarbamol 750 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 85509-1341-3 | 30 TABLET, FILM COATED in 1 BOTTLE (85509-1341-3) | Jul 29, 2025 |
| 85509-1341-6 | 60 TABLET, FILM COATED in 1 BOTTLE (85509-1341-6) | Jul 29, 2025 |
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