Methocarbamol
- Product NDC
- 71610-242
- 11-digit product format
- 716100242
- Labeler code
- 71610
- Product ID
- 71610-242_53b25c9f-5a70-4294-9d8a-abcef0b12211
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71610-242 | METHOCARBAMOL TABLET, FILM COATED [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20190302_3043ecba-d66c-4287-b519-5f9955ac1b18.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-242-53 | 71610024253 | 60 TABLET, FILM COATED in 1 BOTTLE (71610-242-53) | 2019-02-22 | 0000-00-00 | No | No | Current |
| 71610-242-70 | 71610024270 | 120 TABLET, FILM COATED in 1 BOTTLE (71610-242-70) | 2019-02-22 | 0000-00-00 | No | No | Current |
| 71610-242-80 | 71610024280 | 180 TABLET, FILM COATED in 1 BOTTLE (71610-242-80) | 2019-02-22 | 0000-00-00 | No | No | Current |