GLYCOPYRROLATE
- Product NDC
- 69076-475
- 11-digit product format
- 690760475
- Labeler code
- 69076
- Product ID
- 69076-475_f03d88ab-275e-39b2-e053-2a95a90a22a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYCOPYRROLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quinn Pharmaceuticals
- Application
- ANDA091182
- Marketing category
- ANDA
- Marketing start
- 2021-05-01
- Substance
- GLYCOPYRROLATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Anticholinergic [EPC], Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GLYCOPYRROLATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLYCOPYRROLATE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V92SO9WP2I |
| Rxcui | 197738, 197739 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69076-475-01 | GLYCOPYRROLATE | 100 in 1 BOTTLE | TABLET | 100 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69076-475 | GLYCOPYRROLATE TABLET [QUINN PHARMACEUTICALS] | 9 | Current NDC, Legacy NDC, 1 package rows | 20221221_e1ded8e0-c05b-4bf4-a129-57d1726af6ed.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69076-475-01 | 69076047501 | 100 TABLET in 1 BOTTLE (69076-475-01) | 100 tablet | 2021-05-01 | 0000-00-00 | No | No | Current |