Methocarbamol
- Product NDC
- 73352-510
- 11-digit product format
- 733520510
- Labeler code
- 73352
- Product ID
- 73352-510_e250f07b-f60b-4159-a4c2-7470b7a31c69
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Trifluent Pharma LLC
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2025-02-10
- Substance
- METHOCARBAMOL
- Active strength
- 1000 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 | 1000 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 2611794 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73352-510-10 | Methocarbamol | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73352-510 | METHOCARBAMOL TABLET, COATED [TRIFLUENT PHARMA LLC] | 1 | Current NDC, 1 package rows | 20250305_de2e3af9-03ab-4dc8-b480-6866474ad1bd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 73352-510-10 | 73352051010 | 100 TABLET, COATED in 1 BOTTLE (73352-510-10) | 2025-02-10 | No | No | Current |