Methocarbamol
- Product NDC
- 50436-0770
- 11-digit product format
- 504360770
- Labeler code
- 50436
- Product ID
- 50436-0770_6b078e74-3459-48ca-9f79-59160f93c4c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0770-2 | Methocarbamol | 60 in 1 BOTTLE | TABLET, COATED | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0770 | METHOCARBAMOL (METHOCARBAMOL TABLETS) TABLET, COATED [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20181205_6193ff74-cc55-4c99-882b-92a02961b5a5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0770-2 | 50436077002 | 60 in 1 BOTTLE | Historical |