NDC 72789-499 – Methocarbamol Tablets, USP, 500 mg
Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-499
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
- January 1, 2024
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 72789-499-18 | 18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-18) | Apr 16, 2025 |
| 72789-499-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-20) | Apr 28, 2025 |
| 72789-499-28 | 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-28) | Jul 8, 2025 |
Other Methocarbamol Tablets, USP, 500 mg products
- 72162-2487 Methocarbamol 500 mg/1 · Tablet, Film Coated · Bryant Ranch Prepack
- 63561-0173 Methocarbamol 500 mg/1 · Tablet, Film Coated · Granulation Technology, Inc.
- 10135-722 Methocarbamol 500 mg/1 · Tablet, Film Coated · Marlex Pharmaceuticals, Inc.
- 72789-481 Methocarbamol 500 mg/1 · Tablet, Film Coated · PD-Rx Pharmaceuticals, Inc.