NDC 71205-103 – Methocarbamol
Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-103
Product details
- Brand name
- Methocarbamol
- Generic name
- Methocarbamol
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208507
- Marketed since
- January 15, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Methocarbamol 500 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71205-103-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-103-20) | Sep 4, 2018 |
| 71205-103-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-103-30) | Sep 4, 2018 |
| 71205-103-40 | 40 TABLET, FILM COATED in 1 BOTTLE (71205-103-40) | Sep 4, 2018 |
| 71205-103-45 | 45 TABLET, FILM COATED in 1 BOTTLE (71205-103-45) | Sep 4, 2018 |
| 71205-103-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-103-60) | Sep 4, 2018 |
| 71205-103-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-103-90) | Sep 4, 2018 |
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