Methocarbamol
- Product NDC
- 67296-2193
- 11-digit product format
- 672962193
- Labeler code
- 67296
- Product ID
- 67296-2193_4ff1938d-1f5f-0811-e063-6394a90a9049
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA213967
- Marketing category
- ANDA
- Marketing start
- 2023-02-09
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Methocarbamol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHOCARBAMOL | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 197943 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-2193-1 | Methocarbamol | 15 in 1 BOTTLE | TABLET, FILM COATED | 15 | | 2 |
| 67296-2193-2 | Methocarbamol | 24 in 1 BOTTLE | TABLET, FILM COATED | 24 | | 2 |
| 67296-2193-4 | Methocarbamol | 40 in 1 BOTTLE | TABLET, FILM COATED | 40 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2193-1 | 67296219301 | 15 TABLET, FILM COATED in 1 BOTTLE (67296-2193-1) | 2023-02-09 | No | No | Current |
| 67296-2193-2 | 67296219302 | 24 TABLET, FILM COATED in 1 BOTTLE (67296-2193-2) | 2023-02-09 | No | No | Current |
| 67296-2193-4 | 67296219304 | 40 TABLET, FILM COATED in 1 BOTTLE (67296-2193-4) | 2023-02-09 | No | No | Current |