Methocarbamol
- Product NDC
- 45865-987
- 11-digit product format
- 458650987
- Labeler code
- 45865
- Product ID
- 45865-987_9af24216-c452-376c-e053-2a95a90aa613
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- medsource pharmaceuticals
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- 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
- 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 |
|---|
| 45865-987-60 | Methocarbamol | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-987 | METHOCARBAMOL TABLET, FILM COATED [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20191231_9af244ce-8829-4443-e053-2995a90af4e3.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 |
|---|
| 45865-987-60 | 45865098760 | 60 TABLET, FILM COATED in 1 BOTTLE (45865-987-60) | 2019-12-11 | 0000-00-00 | No | No | Current |