Methocarbamol
- Product NDC
- 43063-641
- 11-digit product format
- 430630641
- Labeler code
- 43063
- Product ID
- 43063-641_77bcc15f-a93e-8f63-e053-2a91aa0aaa9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA085159
- Marketing category
- ANDA
- Marketing start
- 2000-01-01
- 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
- 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 |
|---|---|---|---|---|---|
| 43063-641-10 | EA - Each | 43063-641 | 8e3fdf08-5c26-472c-b419-18aa540d6680 | 1 | 2016-09-02 |
| 43063-641-18 | EA - Each | 43063-641 | 75140227-d68b-4bb8-81b2-fde9c0d75365 | 1 | 2016-10-06 |
| 43063-641-20 | EA - Each | 43063-641 | 3a7c7f53-67ea-4f78-ad88-c09a18493b7e | 1 | 2017-05-03 |
| 43063-641-24 | EA - Each | 43063-641 | 73538fbb-99ff-4709-a5c9-eee7449e50ff | 1 | 2017-10-13 |
| 43063-641-28 | EA - Each | 43063-641 | 4a3ea034-a6a5-4d48-9d89-c340dbbd86cd | 1 | 2016-12-07 |
| 43063-641-30 | EA - Each | 43063-641 | 35942aa5-09cd-4939-b330-1a58ae38953b | 1 | 2016-11-08 |
| 43063-641-40 | EA - Each | 43063-641 | 95dd8e2a-fbf6-44e7-b50d-3e5dadfd7332 | 1 | 2016-03-04 |