METHOCARBAMOL
- Product NDC
- 71093-141
- 11-digit product format
- 710930141
- Labeler code
- 71093
- Product ID
- 71093-141_f952d2bf-7825-4a85-9d59-592cbe28d7fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHOCARBAMOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ACI Healthcare USA, Inc.
- Application
- ANDA203550
- Marketing category
- ANDA
- Marketing start
- 2017-02-08
- 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
- 2023-12-31
- 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 |
|---|
| 71093-141-04 | METHOCARBAMOL | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 8 |
| 71093-141-05 | METHOCARBAMOL | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71093-141 | METHOCARBAMOL TABLET, FILM COATED [ACI HEALTHCARE USA, INC.] | 8 | Legacy NDC, 2 package rows | 20231222_b19fe4cb-7a72-4668-8981-db7a1f4fa5a1.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 |
|---|
| 71093-141-04 | 71093014104 | 100 TABLET, FILM COATED in 1 BOTTLE (71093-141-04) | 2017-02-08 | 0000-00-00 | No | No | Current |
| 71093-141-05 | 71093014105 | 500 TABLET, FILM COATED in 1 BOTTLE (71093-141-05) | 2017-02-08 | 0000-00-00 | No | No | Current |