NDC 72789-521 – Methocarbamol Tablets, USP, 750 mg
Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-521
Product details
- Brand name
- Methocarbamol Tablets, USP, 750 mg
- Generic name
- Methocarbamol
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212623
- Marketed since
- June 10, 2025
- Listing expires
- December 31, 2027
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 72789-521-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-20) | Aug 29, 2025 |
| 72789-521-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-30) | Oct 24, 2025 |
| 72789-521-40 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-40) | Mar 23, 2026 |
| 72789-521-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-60) | Sep 18, 2025 |
| 72789-521-82 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-82) | Aug 15, 2025 |
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