Methocarbamol
- Product NDC
- 68071-2867
- 11-digit product format
- 680712867
- Labeler code
- 68071
- Product ID
- 68071-2867_ec95cdba-e227-cd07-e053-2995a90ae04d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68071-2867-6 | Methocarbamol | 6 in 1 BOTTLE | TABLET, COATED | 6 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2867 | METHOCARBAMOL (METHOCARBAMOL TABLETS) TABLET, COATED [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 1 package rows | 20221104_ec95cdba-e226-cd07-e053-2995a90ae04d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2867-6 | 68071286706 | 6 TABLET, COATED in 1 BOTTLE (68071-2867-6) | 2022-11-03 | 0000-00-00 | No | No | Current |