Methocarb 500-EZS
- Product NDC
- 59088-724
- 11-digit product format
- 590880724
- Labeler code
- 59088
- Product ID
- 59088-724_b3ca019e-98e0-1007-e053-2a95a90a1690
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- KIT
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-10-23
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Methocarb 500-EZS
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 197943 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-724-00 | Methocarb 500-EZS | 1 in 1 KIT | KIT | 1 | | 3 |
| 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 |
|---|
| 59088-724 | METHOCARB 500-EZS (METHOCARBAMOL) KIT [PURETEK CORPORATION] | 3 | Current NDC, Legacy NDC, 2 package rows | 20201114_383ce408-1085-43e7-944e-957ff2a9d553.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59088-724-00 | 59088072400 | 1 KIT in 1 KIT (59088-724-00) * 100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10) | 1 kit | 2018-10-23 | 0000-00-00 | No | No | Current |
| 69543-134-10 | 69543013410 | 100 in 1 BOTTLE | | | | | | Historical |