NDC 72789-012 – Methocarbamol
Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-012
Product details
- Brand name
- Methocarbamol
- Generic name
- Methocarbamol
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208507
- Marketed since
- January 15, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Methocarbamol 500 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 72789-012-18 | 18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-18) | Dec 19, 2019 |
| 72789-012-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-20) | Sep 20, 2019 |
| 72789-012-24 | 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-24) | May 5, 2021 |
| 72789-012-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-30) | Aug 10, 2021 |
| 72789-012-40 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40) | Jun 16, 2020 |
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