Metformin Hydrochloride
- Product NDC
- 29033-032
- 11-digit product format
- 290330032
- Labeler code
- 29033
- Product ID
- 29033-032_b80bc941-0d74-4af6-a4b9-b5a2282c1816
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Nostrum Laboratories, Inc.
- Application
- ANDA203832
- Marketing category
- ANDA
- Marketing start
- 2018-01-02
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 29033-032-06 | Metformin Hydrochloride | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED, EXTENDED RE | 60 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29033-032 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [NOSTRUM LABORATORIES, INC.] | 7 | Legacy NDC, 1 package rows | 20240501_17cc4a42-d071-4288-b72e-5c9402f73cff.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 29033-032-06 | 29033003206 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29033-032-06) | 2018-01-02 | 0000-00-00 | No | No | Current |