Methocarbamol
- Product NDC
- 50090-3192
- 11-digit product format
- 500903192
- Labeler code
- 50090
- Product ID
- 50090-3192_e29753cb-7639-4292-99ae-b5c90eca0979
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2015-07-13
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-3192-0 | EA - Each | 50090-3192 | fe38bdf2-bfc0-4ba6-8eee-912261a11db8 | 1 | 2019-05-02 |
| 50090-3192-1 | EA - Each | 50090-3192 | dbdbccf1-098d-42d4-aec2-e49678530da7 | 1 | 2020-02-13 |
| 50090-3192-2 | EA - Each | 50090-3192 | 5df993cd-edcc-44f4-8b7d-03d3bf79e862 | 1 | 2020-02-13 |
| 50090-3192-3 | EA - Each | 50090-3192 | 2aaa5b78-27df-4705-a611-34e9125f9f9a | 1 | 2020-02-13 |
| 50090-3192-4 | EA - Each | 50090-3192 | 60d8131b-040b-462a-aa0c-42fc8bf1ae97 | 1 | 2020-02-13 |
| 50090-3192-6 | EA - Each | 50090-3192 | 9c09c035-ef7b-48c3-93f4-71a934d2d59c | 1 | 2020-02-13 |
| 50090-3192-7 | EA - Each | 50090-3192 | 9010b7af-f163-46c4-a3a3-46ab098bebc8 | 1 | 2020-02-13 |