Methocarbamol
- Product NDC
- 67296-1662
- 11-digit product format
- 672961662
- Labeler code
- 67296
- Product ID
- 67296-1662_b8df9dc5-96b1-e3c0-e053-2a95a90ab769
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2019-01-01
- 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
- 2022-12-31
- 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 |
|---|
| 67296-1662-7 | Methocarbamol | 15 in 1 BOTTLE | TABLET, FILM COATED | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1662 | METHOCARBAMOL TABLET, FILM COATED [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20240806_89175a33-d4c7-c1ef-e053-2a95a90a0fb1.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 |
|---|
| 67296-1662-7 | 67296166207 | 15 TABLET, FILM COATED in 1 BOTTLE (67296-1662-7) | 2019-01-01 | 0000-00-00 | No | No | Current |