Methocarbamol
- Product NDC
- 68151-2775
- 11-digit product format
- 681512775
- Labeler code
- 68151
- Product ID
- 68151-2775_58a8ec19-cbb5-4b77-ace7-03f28be49339
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2013-12-15
- 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
- 2019-12-31
- 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 |
|---|
| 68151-2775-7 | Methocarbamol | 1 in 1 BOTTLE | TABLET, FILM COATED | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2775 | METHOCARBAMOL TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20180215_ca8531bb-4128-4761-98d3-343c786a628d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2775-7 | 68151277507 | 1 in 1 BOTTLE | Historical |