NDC 10135-723 – Methocarbamol Tablets, USP, 750 mg
Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral
Product NDC10135-723
Product details
- Brand name
- Methocarbamol Tablets, USP, 750 mg
- Generic name
- Methocarbamol
- Labeler
- Marlex Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212623
- Marketed since
- December 9, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Methocarbamol 750 mg/1
Uses, dosage, side effects and warnings for Methocarbamol Tablets, USP, 750 mg →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 10135-723-01 | 100 TABLET, FILM COATED in 1 BOTTLE (10135-723-01) | Dec 9, 2021 |
| 10135-723-05 | 500 TABLET, FILM COATED in 1 BOTTLE (10135-723-05) | Dec 9, 2021 |
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