Methocarbamol
- Product NDC
- 63739-991
- 11-digit product format
- 637390991
- Labeler code
- 63739
- Product ID
- 63739-991_c7bc55bf-4d5f-682b-e053-2995a90af285
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2021-07-22
- 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
- 2022-12-31
- 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 |
|---|
| 63739-991 | METHOCARBAMOL (METHOCARBAMOL TABLETS) TABLET, COATED [MCKESSON CORPORATION DBA SKY PACKAGING] | 12 | Legacy NDC | 20250110_c7bc1e92-28cb-31ae-e053-2a95a90aeb3f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-991-10 | 63739099110 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-991-10) > 10 TABLET, COATED in 1 BLISTER PACK | 10 blister pack | 2021-07-22 | 0000-00-00 | No | No | Current |