Methocarbamol
- Product NDC
- 60760-482
- 11-digit product format
- 607600482
- Labeler code
- 60760
- Product ID
- 60760-482_b465e8e9-b2a4-0afb-e053-2a95a90a6299
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2020-11-18
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-482-90 | 60760048290 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-482-90) | 90 tablet | 2020-11-18 | 0000-00-00 | No | No | Current |