Proparacaine Hydrochloride
- Product NDC
- 70518-3408
- 11-digit product format
- 705183408
- Labeler code
- 70518
- Product ID
- 70518-3408_4f067d6e-665e-c24f-e063-6294a90ab03e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Proparacaine Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA080027
- Marketing category
- ANDA
- Marketing start
- 2022-04-08
- Substance
- PROPARACAINE HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Local Anesthesia [PE], Local Anesthetic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Proparacaine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROPARACAINE HYDROCHLORIDE | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U96OL57GOY |
| Rxcui | 1191013 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3408-0 | Proparacaine Hydrochloride | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 7 |
| 70518-3408-0 | Proparacaine Hydrochloride | 15 mL in 1 BOTTLE | SOLUTION/ DROPS | 15 | | 7 |
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 |
|---|
| 70518-3408-0 | 70518340800 | 1 BOTTLE in 1 CARTON (70518-3408-0) / 15 mL in 1 BOTTLE | 1 bottle | 2022-04-08 | 0000-00-00 | No | No | Current |