Metformin Hydrochloride
- Product NDC
- 63187-332
- 11-digit product format
- 631870332
- Labeler code
- 63187
- Product ID
- 63187-332_1b6ac895-7c0d-4464-8a42-a9a16fafcf45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203769
- Marketing category
- ANDA
- Marketing start
- 2014-02-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- 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 |
|---|
| 63187-332 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [PROFICIENT RX LP] | 5 | Legacy NDC | 20210116_afcdbfd7-aed1-4f48-9bac-5a1b04323c61.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-332-00 | 63187033200 | 100 TABLET, FILM COATED in 1 BOTTLE (63187-332-00) | 2014-03-03 | 0000-00-00 | No | No | Current |
| 63187-332-30 | 63187033230 | 30 TABLET, FILM COATED in 1 BOTTLE (63187-332-30) | 2014-03-03 | 0000-00-00 | No | No | Current |
| 63187-332-60 | 63187033260 | 60 TABLET, FILM COATED in 1 BOTTLE (63187-332-60) | 2014-03-03 | 0000-00-00 | No | No | Current |
| 63187-332-90 | 63187033290 | 90 TABLET, FILM COATED in 1 BOTTLE (63187-332-90) | 2014-03-03 | 0000-00-00 | No | No | Current |