Methocarbamol
- Product NDC
- 53002-3590
- 11-digit product format
- 530023590
- Labeler code
- 53002
- Product ID
- 53002-3590_873ebcc4-1f3a-4262-a723-debb26ecc930
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2013-03-20
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-3590 | METHOCARBAMOL TABLET [RPK PHARMACEUTICALS, INC.] | 5 | Legacy NDC, 6 package rows | 20230609_26a25c66-3dc4-4cfa-bd9f-ef3fa068364a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-3590-2 | 53002359002 | 12 BOTTLE in 1 CASE (53002-3590-2) > 20 TABLET in 1 BOTTLE | 12 bottle | 2017-10-01 | 0000-00-00 | No | No | Current |
| 53002-3590-3 | 53002359003 | 12 BOTTLE in 1 CASE (53002-3590-3) > 30 TABLET in 1 BOTTLE | 12 bottle | 2017-10-01 | 0000-00-00 | No | No | Current |
| 53002-3590-4 | 53002359004 | 12 BOTTLE in 1 CASE (53002-3590-4) > 40 TABLET in 1 BOTTLE | 12 bottle | 2017-10-01 | 0000-00-00 | No | No | Current |