ATMEKSI
- Product NDC
- 69528-701
- 11-digit product format
- 695280701
- Labeler code
- 69528
- Product ID
- 69528-701_4ce9560d-185c-1e28-e063-6294a90af77f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Rosemont Pharmaceuticals LLC
- Application
- NDA219843
- Marketing category
- NDA
- Marketing start
- 2025-12-22
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/5mL
- 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
- ATMEKSI
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHOCARBAMOL | 750 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 2729335, 2729341 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69528-701-05 | ATMEKSI | 150 mL in 1 BOTTLE | SUSPENSION | 150 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69528-701-05 | 69528070105 | 150 mL in 1 BOTTLE (69528-701-05) | 150 ml | 2026-01-15 | No | No | Current |