methocarbamol
- Product NDC
- 72887-873
- 11-digit product format
- 728870873
- Labeler code
- 72887
- Product ID
- 72887-873_2d7ed9b4-3cba-fb22-e063-6294a90af27a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- FH2 PHARMA LLC
- Application
- ANDA212707
- Marketing category
- ANDA
- Marketing start
- 2024-08-30
- Substance
- METHOCARBAMOL
- Active strength
- 1000 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 | 1000 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 2611794 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72887-873-03 | methocarbamol | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72887-873 | METHOCARBAMOL TABLET, FILM COATED [FH2 PHARMA LLC] | 2 | Current NDC, 1 package rows | 20250209_1dd56e3d-7ca7-1443-e063-6294a90a13c5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72887-873-03 | 72887087303 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03) | 2024-08-30 | No | No | Historical |