Methocarbamol
- Product NDC
- 70518-4603
- 11-digit product format
- 705184603
- Labeler code
- 70518
- Product ID
- 70518-4603_50849b7b-430c-3631-e063-6294a90a6355
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2026-04-22
- 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 |
|---|
| 70518-4603-0 | Methocarbamol | 40 in 1 BOTTLE, PLASTIC | TABLET, COATED | 40 | | 2 |
| 70518-4603-1 | Methocarbamol | 50 in 1 BOX | TABLET, COATED | 50 | | 2 |
| 70518-4603-2 | Methocarbamol | 1 in 1 POUCH | TABLET, COATED | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4603-0 | 70518460300 | 40 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4603-0) | | 2026-04-22 | No | No | Historical |
| 70518-4603-1 | 70518460301 | 50 POUCH in 1 BOX (70518-4603-1) / 1 TABLET, COATED in 1 POUCH (70518-4603-2) | 50 pouch | 2026-04-27 | No | No | Historical |
| 70518-4603-2 | 70518460302 | 1 in 1 POUCH | | | | | Historical |