Methocarbamol
- Product NDC
- 68071-3859
- 11-digit product format
- 680713859
- Labeler code
- 68071
- Product ID
- 68071-3859_485d986c-7678-9b95-e063-6394a90a43ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 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 | 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 |
|---|
| 68071-3859-2 | Methocarbamol | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 3 |
| 68071-3859-3 | Methocarbamol | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
| 68071-3859-9 | Methocarbamol | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3859-2 | 68071385902 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-3859-2) | 2025-06-04 | No | No | Historical |
| 68071-3859-3 | 68071385903 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3) | 2025-12-24 | No | No | Historical |
| 68071-3859-9 | 68071385909 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3859-9) | 2025-01-14 | No | No | Historical |