METHOCARBAMOL
- Product NDC
- 68788-8880
- 11-digit product format
- 687888880
- Labeler code
- 68788
- Product ID
- 68788-8880_5a48be27-5069-40f3-85de-86f248ae232f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHOCARBAMOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA203550
- Marketing category
- ANDA
- Marketing start
- 2025-06-02
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- METHOCARBAMOL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHOCARBAMOL | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 197943 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8880-3 | 68788888003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8880-3) | 2025-06-02 | No | No | Historical |
| 68788-8880-6 | 68788888006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8880-6) | 2025-06-02 | No | No | Historical |
| 68788-8880-9 | 68788888009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8880-9) | 2025-06-02 | No | No | Historical |