Methocarbamol
- Product NDC
- 72162-1363
- 11-digit product format
- 721621363
- Labeler code
- 72162
- Product ID
- 72162-1363_51c6c6b0-3cfb-445a-bde4-0fedf48c18b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA086989
- Marketing category
- ANDA
- Marketing start
- 2017-12-15
- Substance
- METHOCARBAMOL
- Active strength
- 500 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 | 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 |
|---|
| 72162-1363-1 | Methocarbamol | 100 in 1 BOTTLE | TABLET | 100 | | 100 |
| 72162-1363-5 | Methocarbamol | 500 in 1 BOTTLE | TABLET | 500 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1363 | METHOCARBAMOL TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20240206_8cf27774-82ed-4ed1-a55d-41bf476745db.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1363-1 | 72162136301 | 100 TABLET in 1 BOTTLE (72162-1363-1) | 100 tablet | 2024-02-05 | No | No | Historical |
| 72162-1363-5 | 72162136305 | 500 TABLET in 1 BOTTLE (72162-1363-5) | 500 tablet | 2024-02-05 | No | No | Historical |