Methocarbamol Tablets, USP, 750 mg
- Product NDC
- 63561-0174
- 11-digit product format
- 635610174
- Labeler code
- 63561
- Product ID
- 63561-0174_35c0e9af-ba8b-0416-e063-6294a90a87f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Granulation Technology, Inc.
- Application
- ANDA212623
- Marketing category
- ANDA
- Marketing start
- 2025-06-10
- 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 Tablets, USP, 750 mg
- 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 | 197943, 197944 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 63561-0174-1 | 2025-02-07 | C162847 | 48780-1 | 2cef2736-730a-d83d-e063-dadaa90ab31f | Methocarbamol Tablets, USP, 500 mg and 750 mg |
| 63561-0174-5 | 2025-02-07 | C162847 | 48780-1 | 2cef2736-730a-d83d-e063-dadaa90ab31f | Methocarbamol Tablets, USP, 500 mg and 750 mg |
| 63561-0174-1 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-730a-d83d-e063-dadaa90ab31f | Methocarbamol Tablets, USP, 500 mg and 750 mg |
| 63561-0174-5 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-730a-d83d-e063-dadaa90ab31f | Methocarbamol Tablets, USP, 500 mg and 750 mg |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63561-0174-1 | Methocarbamol Tablets, USP, 750 mg | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 3 |
| 63561-0174-5 | Methocarbamol Tablets, USP, 750 mg | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63561-0174 | METHOCARBAMOL TABLETS, USP, 500 MG (METHOCARBAMOL) TABLET, FILM COATED METHOCARBAMOL TABLETS, USP, 750 MG (METHOCARBAMOL) TABLET, FILM COATED [GRANULATION TECHNOLOGY, INC.] | 2 | Current NDC, 2 package rows | 20250210_70c5342c-9597-4fe6-863c-f8ae4adc063a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 63561-0174-1 | 63561017401 | 100 TABLET, FILM COATED in 1 BOTTLE (63561-0174-1) | 2025-06-10 | No | No | Current |
| 63561-0174-5 | 63561017405 | 500 TABLET, FILM COATED in 1 BOTTLE (63561-0174-5) | 2025-06-10 | No | No | Current |