Methocarbamol
- Product NDC
- 85509-1341
- 11-digit product format
- 855091341
- Labeler code
- 85509
- Product ID
- 85509-1341_3b19915a-94cf-d115-e063-6394a90a7aa3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PHOENIX RX LLC
- Application
- ANDA213967
- Marketing category
- ANDA
- Marketing start
- 2020-08-12
- Substance
- METHOCARBAMOL
- Active strength
- 750 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 | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 197944 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85509-1341-3 | Methocarbamol | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 85509-1341-6 | Methocarbamol | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 85509-1341-3 | 85509134103 | 30 TABLET, FILM COATED in 1 BOTTLE (85509-1341-3) | 2025-07-29 | No | No | Historical |
| 85509-1341-6 | 85509134106 | 60 TABLET, FILM COATED in 1 BOTTLE (85509-1341-6) | 2025-07-29 | No | No | Historical |