Methocarbamol
- Product NDC
- 69543-134
- 11-digit product format
- 695430134
- Labeler code
- 69543
- Product ID
- 69543-134_80d903de-b812-478c-8124-95a9dc55f1a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Virtus Pharmaceuticals
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2015-07-13
- Marketing end
- 2020-10-31
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69543-134-10 | Methocarb 500-EZS | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 500 mg | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69543-134 | METHOCARB 500-EZS (METHOCARBAMOL) KIT [PURETEK CORPORATION] | 3 | Legacy NDC | 20201114_383ce408-1085-43e7-944e-957ff2a9d553.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69543-134-10 | 69543013410 | 100 in 1 BOTTLE | Historical |