NDC 87063-040 – Methocarbamol
Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral
Product NDC87063-040
Product details
- Brand name
- Methocarbamol
- Generic name
- Methocarbamol
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213967
- Marketed since
- February 9, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Methocarbamol 500 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 87063-040-01 | 100 TABLET, FILM COATED in 1 BOTTLE (87063-040-01) | Nov 24, 2025 |
| 87063-040-10 | 10 TABLET, FILM COATED in 1 BOTTLE (87063-040-10) | Nov 24, 2025 |
| 87063-040-20 | 20 TABLET, FILM COATED in 1 BOTTLE (87063-040-20) | Nov 24, 2025 |
| 87063-040-30 | 30 TABLET, FILM COATED in 1 BOTTLE (87063-040-30) | Nov 24, 2025 |
| 87063-040-60 | 60 TABLET, FILM COATED in 1 BOTTLE (87063-040-60) | Nov 24, 2025 |
| 87063-040-90 | 90 TABLET, FILM COATED in 1 BOTTLE (87063-040-90) | Nov 24, 2025 |
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