Methocarbamol
- Product NDC
- 53002-3592
- 11-digit product format
- 530023592
- Labeler code
- 53002
- Product ID
- 53002-3592_f0c49b81-91d5-4752-aa70-0d82a64edfb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- 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
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-3592-2 | 53002359202 | 20 TABLET, FILM COATED in 1 BOTTLE (53002-3592-2) | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-3592-3 | 53002359203 | 30 TABLET, FILM COATED in 1 BOTTLE (53002-3592-3) | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-3592-4 | 53002359204 | 40 TABLET, FILM COATED in 1 BOTTLE (53002-3592-4) | 2019-01-01 | 0000-00-00 | No | No | Current |