NDC 72789-481 – Methocarbamol Tablets, USP, 500 mg
Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-481
Product details
- Brand name
- Methocarbamol Tablets, USP, 500 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, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Methocarbamol 500 mg/1
Uses, dosage, side effects and warnings for Methocarbamol Tablets, USP, 500 mg →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 72789-481-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-01) | Jun 10, 2025 |
| 72789-481-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-30) | Sep 3, 2025 |
| 72789-481-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-60) | Jun 10, 2025 |
| 72789-481-82 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-82) | Jun 10, 2025 |
| 72789-481-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-90) | Jun 10, 2025 |
| 72789-481-93 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-93) | Jun 10, 2025 |
| 72789-481-95 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-95) | Jun 10, 2025 |
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