METHOCARBAMOL
- Product NDC
- 61919-627
- 11-digit product format
- 619190627
- Labeler code
- 61919
- Product ID
- 61919-627_87388b8c-daa4-3fbb-e053-2a91aa0a3e9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHOCARBAMOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- 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
- 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 |
|---|
| 61919-627-90 | METHOCARBAMOL | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-627 | METHOCARBAMOL TABLET, FILM COATED METHOCARBAMOL TABLET, COATED METHOCARBAMOL TABLET [DIRECTRX] | 4 | Legacy NDC, 1 package rows | 20190424_270b68a6-1469-190d-e054-00144ff8d46c.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 |
|---|
| 61919-627-90 | 61919062790 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-627-90) | 2015-01-01 | 0000-00-00 | No | No | Current |