NDC 72789-021 – Methocarbamol
Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-021
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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 72789-021-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-01) | Oct 24, 2019 |
| 72789-021-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-60) | Sep 12, 2023 |
| 72789-021-82 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-82) | Oct 24, 2019 |
| 72789-021-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-90) | Sep 12, 2023 |
| 72789-021-93 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-93) | Oct 24, 2019 |
| 72789-021-94 | 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-94) | Oct 24, 2019 |
| 72789-021-99 | 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-99) | Oct 24, 2019 |
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